Estudio del defecto familiar de unión de la apolipoproteína B100 en una población mediterránea-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Estudio del defecto familiar de unión de la apolipoproteína B100 en una población mediterránea

Published:2004-10 Issue:12 Volume:123 Page:456-459
ISSN:0025-7753
Container-title:Medicina Clínica
language:es
Short-container-title:Medicina Clínica

Author:

Ejarque Ismael,Real José T.,Chaves Felipe J.,Blesa Sebastián,González Verónica,Milian Enrique,Ascaso Juan F.,Priego María A.,Carmena Rafael

Publisher

Elsevier BV

Subject

General Medicine

Reference31 articles.

1. Familial defective apolipoprotein B- 100 a review, including some comparison with familial hypercholesterolemia;Myant;Atherosclerosis,1993

2. Familial defective apolipoprotein B-100: a common cause of primary hypercholesterolemia;Rauh;Clin Investig,1992

3. Familial ligand-defective apolipoprotein B: identification of a new mutation that decreases LDL receptor binding affinity;Pullinger;J Clin Invest,1995

4. Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidaemia;Gaffney;Arterioscle Thromb Vasc Biol,1995

5. Familial hypercholesterolemia;Goldstein,2001

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP